US9782463B2ExpiredUtilityA1

Method for allogeneic cell therapy

Assignee: IMMUNOVATIVE THEARPIES LTDPriority: May 13, 2003Filed: Feb 11, 2016Granted: Oct 10, 2017
Est. expiryMay 13, 2023(expired)· nominal 20-yr term from priority
Inventors:Michael Har-Noy
C12N 2531/00C12N 2533/40A61P 37/06A61P 35/00C12N 2501/515A61P 31/00A61P 33/00C12N 2501/51A61K 2039/57A61P 31/12A61P 37/04A61K 39/0005A61P 37/02C12N 5/0636A61K 35/17A61K 2039/5154A61K 40/50A61K 40/42A61K 40/30A61K 40/15A61K 40/11
95
PatentIndex Score
8
Cited by
189
References
4
Claims

Abstract

A method of manipulating allogeneic cells for use in allogeneic cell therapy providing a composition of highly activated allogeneic T-cells which are infused into immunocompetent cancer patients to elicit a novel anti-tumor immune mechanism, or “Mirror Effect”. In contrast to current allogeneic cell therapy protocols where T-cells in the graft mediate the beneficial graft vs. tumor (GVT) and detrimental graft vs. host (GVH) effects, the allogeneic cells of the present invention stimulate host T-cells to mediate the “mirror” of these effects. The mirror of the GVT effect is the host vs. tumor (HVT) effect. The “mirror” of the GVH effect is the host vs. graft (HVG) effect The anti-tumor HVT effect occurs in conjunction with a non-toxic HVG rejection effect. The highly activated allogeneic cells of the invention can be used to stimulate host immunity in a complete HLA mis-matched setting in a patient.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method for stimulating a host immune response against a tumor comprising:
 selecting cells from a normal donor of which at least a portion are T-cells; 
 activating and formulating said donor cells ex vivo in media suitable for infusion into a host cancer patient, wherein said cells are activated by CD3 and CD28 surface antigen cross-linking; and 
 administering said activated donor cells to the host who has a 50% or less tissue match to said normal donor. 
 
     
     
       2. The method of  claim 1  wherein the host immune response against the tumor includes the production of a “cytokine storm” including at least one of the following cytokines: IL-2, IL-15, TNF-alpha, TNF-beta, IL-12 and IFN-gamma. 
     
     
       3. The method of  claim 2  wherein the selected normal donor cells are frozen prior to activation. 
     
     
       4. The method of  claim 1  wherein the host immune response against the tumor includes activating innate cells including NK cells or macrophages.

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